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This unique book on super-resolution microscopy techniques presents comparative, in-depth analyses of the strengths and weaknesses of the individual approaches. It was written for non-experts who need to understand the principles of super-resolution or who wish to use recently commercialized instruments as well as for professionals who plan to realize novel microscopic devices. Explaining the practical requirements in terms of hardware, software and sample preparation, the book offers a wealth of hands-on tips and practical tricks to get a setup running, provides invaluable help and support…mehr
This unique book on super-resolution microscopy techniques presents comparative, in-depth analyses of the strengths and weaknesses of the individual approaches. It was written for non-experts who need to understand the principles of super-resolution or who wish to use recently commercialized instruments as well as for professionals who plan to realize novel microscopic devices. Explaining the practical requirements in terms of hardware, software and sample preparation, the book offers a wealth of hands-on tips and practical tricks to get a setup running, provides invaluable help and support for successful data acquisition and specific advice in the context of data analysis and visualization. Furthermore, it addresses a wide array of transdisciplinary fields of applications. The author begins by outlining the joint efforts that have led to achieving super-resolution microscopy combining advances in single-molecule photo-physics, fluorophore design and fluorescent labeling, instrument design and software development. The following chapters depict and compare current main standard techniques such as structured illumination microscopy, single-molecule localization, stimulated emission depletion microscopy and multi-scale imaging including light-sheet and expansion microscopy. For each individual approach the experimental setups are introduced, the imaging protocols are provided and the various applications illustrated. The book concludes with a discussion of future challenges addressing issues of routine applications and further commercialization of the available methods. Guiding users in how to make choices for the design of their own experiments from scratch to promising application, this one-stop resource is intended for researchers in the applied sciences, from chemistry to biology and medicine to physics and engineering.
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Autorenporträt
Udo Birk studied physics and mathematics in Canada and Germany and obtained a PhD in applied physics from the University of Heidelberg (Germany) for his work on tissue spectrometry and spatially modulated illumination microscopy. He was a Marie-Curie Fellow at King's College London (UK) and at the Foundation of Research and Technology Hellas (Greece), where he worked on structured illumination microscopy and on optical projection tomography. Currently, he is deputy group leader at the Institute of Molecular Biology in Mainz (Germany), which equals a position of an associate professor, and his research focuses on the development and application of advanced optical imaging techniques.
Inhaltsangabe
Preface Abbreviations
INTRODUCTION The Classical Resolution Limit Methods to Circumvent the Classical Resolution Barrier in Fluorescence Microscopy Implementation of Super-Resolution Microscopy (SRM) Contrast Applications to Study Nuclear DNA Other Applications
PHYSICOCHEMICAL BACKGROUND Motivation Labeling Transitions of the Fluorophores Samples
HARD- AND SOFTWARE Hardware Requirements Software Open Source and Best Practice
LOCALIZATION MICROSCOPY On the Principles of Localization Microscopy PALM/STORM/fPALM/SPDM Approach Implementation of SMLM On the Principles of Three-Dimensional SMLM Reduction of Out-of-Focus Light How to Build a Three-Dimensional SMLM High-Density Single Emitter Microscopy Methods: SOFI, 3B, SHRImP, etc. Approaches Towards Counting Molecules Requirements and Sample Preparation Data Acquisition Data Analysis Troubleshooting Meta Analysis Tailored for SMLM Example Applications
STIMULATED EMISSION DEPLETION MICROSCOPY (STED) On the Principles of Stimulated Emission Depletion Microscopy Implementation of STED Fluorescent Probes Dye Combinations for Dual-Color STED Requirements and Sample Preparation Data Acquisition Data Analysis and Visualization Example Applications Conclusion
MULTI-SCALE IMAGING Light-Sheet Fluorescence Microscopy (LSFM) Optical Projection Tomography (OPT) Expansion Microscopy (ExM) and Sample Clearing Alternative Approaches
DISCUSSION Future Challenges Commercialization of Super-Resolution Microscopes Concluding Remarks
INTRODUCTION The Classical Resolution Limit Methods to Circumvent the Classical Resolution Barrier in Fluorescence Microscopy Implementation of Super-Resolution Microscopy (SRM) Contrast Applications to Study Nuclear DNA Other Applications
PHYSICOCHEMICAL BACKGROUND Motivation Labeling Transitions of the Fluorophores Samples
HARD- AND SOFTWARE Hardware Requirements Software Open Source and Best Practice
LOCALIZATION MICROSCOPY On the Principles of Localization Microscopy PALM/STORM/fPALM/SPDM Approach Implementation of SMLM On the Principles of Three-Dimensional SMLM Reduction of Out-of-Focus Light How to Build a Three-Dimensional SMLM High-Density Single Emitter Microscopy Methods: SOFI, 3B, SHRImP, etc. Approaches Towards Counting Molecules Requirements and Sample Preparation Data Acquisition Data Analysis Troubleshooting Meta Analysis Tailored for SMLM Example Applications
STIMULATED EMISSION DEPLETION MICROSCOPY (STED) On the Principles of Stimulated Emission Depletion Microscopy Implementation of STED Fluorescent Probes Dye Combinations for Dual-Color STED Requirements and Sample Preparation Data Acquisition Data Analysis and Visualization Example Applications Conclusion
MULTI-SCALE IMAGING Light-Sheet Fluorescence Microscopy (LSFM) Optical Projection Tomography (OPT) Expansion Microscopy (ExM) and Sample Clearing Alternative Approaches
DISCUSSION Future Challenges Commercialization of Super-Resolution Microscopes Concluding Remarks
Index
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